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Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite
The aims of this study were to: (1) synthesize an anti-biofilm and protein-repellent dental composite by combining 2-methacryloyloxyethyl phosphorylcholine (MPC) with quaternary ammonium dimethylaminohexadecyl methacrylate (DMAHDM); and (2) evaluate the effects of water-aging for 180 days on protein...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297818/ https://www.ncbi.nlm.nih.gov/pubmed/28106774 http://dx.doi.org/10.3390/ijms18010186 |
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author | Zhang, Ning Zhang, Ke Melo, Mary A. S. Weir, Michael D. Xu, David J. Bai, Yuxing Xu, Hockin H. K. |
author_facet | Zhang, Ning Zhang, Ke Melo, Mary A. S. Weir, Michael D. Xu, David J. Bai, Yuxing Xu, Hockin H. K. |
author_sort | Zhang, Ning |
collection | PubMed |
description | The aims of this study were to: (1) synthesize an anti-biofilm and protein-repellent dental composite by combining 2-methacryloyloxyethyl phosphorylcholine (MPC) with quaternary ammonium dimethylaminohexadecyl methacrylate (DMAHDM); and (2) evaluate the effects of water-aging for 180 days on protein resistance, bacteria-killing ability, and mechanical properties of MPC-DMAHDM composite. MPC and DMAHDM were added into a resin composite. Specimens were stored in distilled water at 37 °C for 1, 30, 90, and 180 days. Mechanical properties were measured in three-point flexure. Protein attachment onto the composite was evaluated by a micro bicinchoninic acid approach. An oral plaque microcosm biofilm model was employed to evaluate oral biofilm viability vs. water-aging time. Mechanical properties of the MPC-DMAHDM composite after 180-day immersion matched those of the commercial control composite. The composite with 3% MPC + 1.5% DMAHDM had much stronger resistance to protein adhesion than control (p < 0.05). MPC + DMAHDM achieved much stronger biofilm-eradicating effects than MPC or DMAHDM alone (p < 0.05). Biofilm colony-forming units on the 3% MPC + 1.5% DMAHDM composite were three orders of magnitude lower than commercial control. The protein-repellent and antibacterial effects were durable and showed no loss in water-aging from 1 to 180 days. The novel MPC-DMAHDM composite possessed strong and durable resistance to protein adhesion and potent bacteria-eradicating function, while matching the load-bearing ability of a commercial dental composite. The novel MPC-DMAHDM composite represents a promising means of suppressing oral plaque growth, acid production, and secondary caries. |
format | Online Article Text |
id | pubmed-5297818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-52978182017-02-10 Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite Zhang, Ning Zhang, Ke Melo, Mary A. S. Weir, Michael D. Xu, David J. Bai, Yuxing Xu, Hockin H. K. Int J Mol Sci Article The aims of this study were to: (1) synthesize an anti-biofilm and protein-repellent dental composite by combining 2-methacryloyloxyethyl phosphorylcholine (MPC) with quaternary ammonium dimethylaminohexadecyl methacrylate (DMAHDM); and (2) evaluate the effects of water-aging for 180 days on protein resistance, bacteria-killing ability, and mechanical properties of MPC-DMAHDM composite. MPC and DMAHDM were added into a resin composite. Specimens were stored in distilled water at 37 °C for 1, 30, 90, and 180 days. Mechanical properties were measured in three-point flexure. Protein attachment onto the composite was evaluated by a micro bicinchoninic acid approach. An oral plaque microcosm biofilm model was employed to evaluate oral biofilm viability vs. water-aging time. Mechanical properties of the MPC-DMAHDM composite after 180-day immersion matched those of the commercial control composite. The composite with 3% MPC + 1.5% DMAHDM had much stronger resistance to protein adhesion than control (p < 0.05). MPC + DMAHDM achieved much stronger biofilm-eradicating effects than MPC or DMAHDM alone (p < 0.05). Biofilm colony-forming units on the 3% MPC + 1.5% DMAHDM composite were three orders of magnitude lower than commercial control. The protein-repellent and antibacterial effects were durable and showed no loss in water-aging from 1 to 180 days. The novel MPC-DMAHDM composite possessed strong and durable resistance to protein adhesion and potent bacteria-eradicating function, while matching the load-bearing ability of a commercial dental composite. The novel MPC-DMAHDM composite represents a promising means of suppressing oral plaque growth, acid production, and secondary caries. MDPI 2017-01-18 /pmc/articles/PMC5297818/ /pubmed/28106774 http://dx.doi.org/10.3390/ijms18010186 Text en © 2017 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Ning Zhang, Ke Melo, Mary A. S. Weir, Michael D. Xu, David J. Bai, Yuxing Xu, Hockin H. K. Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title | Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title_full | Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title_fullStr | Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title_full_unstemmed | Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title_short | Effects of Long-Term Water-Aging on Novel Anti-Biofilm and Protein-Repellent Dental Composite |
title_sort | effects of long-term water-aging on novel anti-biofilm and protein-repellent dental composite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297818/ https://www.ncbi.nlm.nih.gov/pubmed/28106774 http://dx.doi.org/10.3390/ijms18010186 |
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